NUP98 Rearrangement in Acute Myelomonocytic Leukemia With t(11;19)(p15;p12): The First Case Report Worldwide

Dear Editor, AML is a group of heterogeneous diseases derived from various cytogenetic and molecular abnormalities that are significant for diagnosis, treatment, and prognosis in many cases. We report a rare case of AML harboring t(11;19)(p15;p12) that was detected with whole-genome sequencing (WGS)...

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Veröffentlicht in:	Annals of laboratory medicine 2017, 37(3), , pp.285-287
Hauptverfasser:	Lim, Hyeon Ho, An, Gyu Dae, Woo, Kwang Sook, Kim, Kyeong Hee, Kim, Jeong Man, Kim, Sung Hyun, Han, Jin Yeong
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Bone Marrow - pathology Chromosomes, Human, Pair 11 Chromosomes, Human, Pair 19 Female Humans Karyotype Letter to the Editor Leukemia, Myelomonocytic, Acute - diagnosis Leukemia, Myelomonocytic, Acute - genetics Nuclear Pore Complex Proteins - genetics Translocation, Genetic Whole Genome Sequencing 병리학
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Zusammenfassung:	Dear Editor, AML is a group of heterogeneous diseases derived from various cytogenetic and molecular abnormalities that are significant for diagnosis, treatment, and prognosis in many cases. We report a rare case of AML harboring t(11;19)(p15;p12) that was detected with whole-genome sequencing (WGS). KCI Citation Count: 1
ISSN:	2234-3806 2234-3814
DOI:	10.3343/alm.2017.37.3.285